HGVS | Genome Assembly |
---|---|
NC_000014.9:g.75008985_75008988del , CM000676.2:g.75008985_75008988del | GRCh38 |
NC_000014.8:g.75475688_75475691del , CM000676.1:g.75475688_75475691del | GRCh37 |
NC_000014.7:g.74545441_74545444del | NCBI36 |
NG_013333.1:g.11077_11080del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266126.10:c.899-46_899-43del MANE Select | ENSP00000266126.5:n.899-46_899-43del | |
ENST00000266126.9:c.899-46_899-43del | ENSP00000266126.5:n.899-46_899-43del | |
ENST00000556668.1:n.479-46_479-43del | ||
NM_014239.3:c.899-46_899-43del | NP_055054.1:n.899-46_899-43del | |
NM_014239.4:c.899-46_899-43del MANE Select | NP_055054.1:n.899-46_899-43del |